Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alicia, Gates"'
Autor:
Zhenfeng Xu, Gregory D. Ford, DaJoie R. Croslan, Ju Jiang, Alicia Gates, Robert Allen, Byron D. Ford
Publikováno v:
Neurobiology of Disease, Vol 19, Iss 3, Pp 461-470 (2005)
Neuregulins are a family of growth factors with potent neuroprotective properties. We recently demonstrated that neuregulin-1 blocked delayed neuronal death following focal ischemic stroke in the rat. Focal ischemia results in the release of pro-infl
Externí odkaz:
https://doaj.org/article/2dbb8065cf3d40fb8eef5a512ca600e0
Autor:
Zhenfeng Xu, Gregory D. Ford, DaJoie R. Croslan, Ju Jiang, Alicia Gates, Robert Allen, Byron D. Ford
Publikováno v:
Neurobiology of Disease, Vol 31, Iss 2, Pp 286- (2008)
Externí odkaz:
https://doaj.org/article/703bb966f1d04625b75249f9a23cd0f4
Autor:
Alicia Gates, Todd E. White, Michelle C. LaPlaca, Benem-Orom Davids, Byron D. Ford, Monique C. Surles-Zeigler, Timothy J. Distel, Gregory D. Ford
Publikováno v:
White, TE; Surles-Zeigler, MC; Ford, GD; Gates, AS; Davids, B; Distel, T; et al.(2016). Bilateral gene interaction hierarchy analysis of the cell death gene response emphasizes the significance of cell cycle genes following unilateral traumatic brain injury. BMC GENOMICS, 17. doi: 10.1186/s12864-016-2412-0. UC Riverside: Retrieved from: http://www.escholarship.org/uc/item/7w48r1rw
BMC genomics, vol 17, iss 1
BMC Genomics
BMC genomics, vol 17, iss 1
BMC Genomics
Background Delayed or secondary cell death that is caused by a cascade of cellular and molecular processes initiated by traumatic brain injury (TBI) may be reduced or prevented if an effective neuroprotective strategy is employed. Microarray and subs
Autor:
Mika A.B. Matthews, Ernest C. Steele, Darryl B. Hood, Alicia Gates, Gregory D. Ford, Byron D. Ford, Sophia Mirza, Peter R. MacLeish
Publikováno v:
Biochemical and Biophysical Research Communications. 377:556-561
The Purkinje cell degeneration (PCD) mutant mouse is characterized by a degeneration of cerebellar Purkinje cells and progressive ataxia. To identify the molecular mechanisms that lead to the death of Purkinje neurons in PCD mice, we used Affymetrix
Autor:
Matthew C. Schoell, Byron D. Ford, DaJoie R. Croslan, Alicia Gates, Adalynn E. Harris, Gregory D. Ford, John V.K. Pulliam, Ceilessia M. Clement
Publikováno v:
Brain Research. 1210:39-47
We previously showed that neuregulin-1 (NRG-1) protected neurons from death in vivo following focal ischemia. The goal of this study was to develop an in vitro rat ischemia model to examine the cellular and molecular mechanisms involved in the neurop
Autor:
Gregory D. Ford, Byron D. Ford, Alicia Gates, Robert Allen, Ju Jiang, DaJoie R. Croslan, Zhenfeng Xu
Publikováno v:
Neurobiology of Disease, Vol 19, Iss 3, Pp 461-470 (2005)
Neuregulins are a family of growth factors with potent neuroprotective properties. We recently demonstrated that neuregulin-1 blocked delayed neuronal death following focal ischemic stroke in the rat. Focal ischemia results in the release of pro-infl
Autor:
Gregory D. Ford, Michelle C. LaPlaca, Byron D. Ford, Todd E. White, Monique C. Surles-Zeigler, Alicia Gates
Publikováno v:
BMC Genomics
BMC genomics, vol 14, iss 1
BMC genomics, vol 14, iss 1
Background Traumatic brain injury (TBI) results in irreversible damage at the site of impact and initiates cellular and molecular processes that lead to secondary neural injury in the surrounding tissue. We used microarray analysis to determine which
Autor:
Gregory D. Ford, DaJoie R. Croslan, Ju Jiang, Robert Allen, Alicia Gates, Byron D. Ford, Zhenfeng Xu
Publikováno v:
Neurobiology of Disease, Vol 31, Iss 2, Pp 286-(2008)
Publikováno v:
Journal of Molecular Signaling
Muscarinic acetylcholine receptors (mAChRs) undergo agonist-promoted internalization, but evidence suggesting that the mechanism of internalization is beta-arrestin dependent has been contradictory and unclear. Previous studies using heterologous ove
Publikováno v:
Brain research. 1071(1)
To gain greater insight on the molecular mechanisms that underlie ischemic stroke, we compared gene expression profiles in transient (tMCAO) and permanent middle cerebral artery occlusion (pMCAO) stroke models using Expression Analysis Systematic Exp